FDA Inspection 1096141 — Solesence, Inc.

Solesence, Inc. — FEI 3003574860

The FDA completed an inspection of Solesence, Inc. on June 7, 2019 in Romeoville, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 7, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Romeoville, IL (United States)